T/C3D 002-2023 Active Group standards

T/C3D 002-2023 Medical display testing and evaluation specification

Publish Date: 2023-04-28 Implement Date: 2023-05-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

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Basic Information

Standard Code: T/C3D 002-2023

Standard Type: Group standards

Standard Status: Active

is_force_gb: no

CCS Name: -

ICS Name: Integrated medical equipment

Publish Date: 2023-04-28

Implement Date: 2023-05-01

Scope

Scope: This document specifies the display technology requirements and testing authorization process for medical displays. This document applies to the design, production, testing, and application of ultra-high-definition medical displays. Main technical content: Medical displays are platforms for presenting digital medical images. They are display devices specifically designed for various medical imaging diagnosis and treatment, as well as information management purposes. They are also display units used in applications involving medical image acquisition, processing, storage, display, transmission, browsing, diagnosis, treatment, teaching, and training. The technology of medical displays is constantly evolving. Different applications of medical displays have different special requirements. To promote the Combined Medical and Industrial Health Action and ensure that medical displays meet health requirements, it is necessary to establish technical requirements and testing evaluation standards for medical displays with different applications.

Development Information

Related Standards

GB/T 16886.11-1997 Replaced

GB/T 16886.11-1997 Biological evaluation of medical devices—Part 11:Tests for systemic toxicity

Publish Date: 1997-06-26

GB/T 16886.3-1997 Replaced

GB/T 16886.3-1997 Biological evaluation of medical devices—Part 3:Tests for genotoxicity, carcinogenicity and reproductive toxicity

Publish Date: 1997-06-26

GB/T 16886.6-1997 Replaced

GB/T 16886.6-1997 Biological evaluation of medical devices—Part 6:Tests for local effects after implantation

Publish Date: 1997-06-26

GB/T 16886.1-2001 Replaced

GB/T 16886.1-2001 Biological evaluation of medical devices—Part 1:Evaluation and testing

Publish Date: 2001-09-24

GB/T 16886.13-2001 Replaced

GB/T 16886.13-2001 Biological evaluation of medical devices—Part 13:Identification and quantification of degradation products from polymeric medical devices

Publish Date: 2001-09-24

GB/T 16886.7-2001 Replaced

GB/T 16886.7-2001 Biological evaluation of medical devices—Part 7:Ethylene oxide sterilization residuals

Publish Date: 2001-09-24